CV Lattes
ORCID
Abstract
Rett syndrome (Rett syndrome, RS) is a rare genetic disease, with an estimated global incidence of 1: 15,000 live births in the female sex. Clinically, it is a neurodevelopmental disease characterized by normal development until 6 to 18 months followed by a period of developmental delay, subsequent rapid regression, a pseudo-stationary period and slow deterioration. People with RS will re…